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This week, the FDA posted a blog post about that meeting, emphasizing its "renewed unwavering commitment to the rare disease community." Advisors on FDA's Vaccines and Related Biological Products Advisory Committee are meeting on Thursday, 18 June, to discuss whether to recommend approval of Moderna's MFLUSIVA mRNA influenza vaccine for adults ages 5064 and accelerated approval for adults 65 and older

Furin cleavage of PA results in its oligomerization at the cell surface into a pre-pore that facilitates membrane interactions with edema factor and lethal factor

Introduction: Why Compare Oral and Injectable BPC-157

However, "safer" and "better" are not the same thing